Structure–activity relationships of analogues of NF449 confirm NF449 as the most potent and selective known P2X1 receptor antagonist
- 30 April 2004
- journal article
- research article
- Published by Elsevier in European Journal of Medicinal Chemistry
- Vol. 39 (4), 345-357
- https://doi.org/10.1016/j.ejmech.2004.01.007
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Identification of a Novel Human ADP Receptor Coupled to GiJournal of Biological Chemistry, 2001
- A G Protein-coupled Receptor for UDP-glucoseJournal of Biological Chemistry, 2000
- Pharmacology of Cloned P2X ReceptorsAnnual Review of Pharmacology and Toxicology, 2000
- The novel pyridoxal-5′-phosphate derivative PPNDS potently antagonizes activation of P2X1 receptorsEuropean Journal of Pharmacology, 2000
- Pharmacological characterization of the human P2Y11 receptorBritish Journal of Pharmacology, 1999
- Sulfanilic Acid-, Benzenedisulfonic Acid-, and Naphthalenetrisulfonic Acid AnaloguesArchiv der Pharmazie, 1998
- Vasoconstrictor responses via P2X‐receptors are selectively antagonized by NF023 in rabbit isolated aorta and saphenous arteryBritish Journal of Pharmacology, 1997
- Evidence for the presence of two types of P2 purinoceptor in the guinea-pig ileal longitudinal smooth muscle preparationEuropean Journal of Pharmacology, 1994
- Purinoceptors: Are there families of P2X and P2Y purinoceptors?Pharmacology & Therapeutics, 1994
- PPADS, a novel functionally selective antagonist of P2 purinoceptor-mediated responsesEuropean Journal of Pharmacology, 1992